Evidence map›Paper›PMID 34618999›Full record

ArticleMolecular oncology2022

USP35 mitigates endoplasmic reticulum stress-induced apoptosis by stabilizing RRBP1 in non-small cell lung cancer.

Wenqing Wang, Meixia Wang, Yi Xiao, Yige Wang, Lijuan Ma, Lulu Guo, Xinyue Wu, Xiaoyan Lin, Pengju Zhang

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.9field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. USP35 Acts as a Deubiquitinating Enzyme for ID3 to Promote Immune Escape in Colorectal Cancer.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  3. Article
  4. Article
  5. Review
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  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Endoplasmic reticulum stress in non-small cell lung cancer.American journal of cancer research · 2025
    Review
  16. Article
  17. Article
  18. Genomic alterations in oral multiple primary cancers.International journal of oral science · 2024
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 1 institution in 2 countries.

Wenqing WangDepartment of Biochemistry and Molecular Biology, Shandong University School of Basic Medical Sciences, Jinan, China.
Meixia WangDepartment of Internal Medicine, Qingdao Fuwai Cardiovascular Hospital, China.
Yi XiaoDepartment of Biochemistry and Molecular Biology, Shandong University School of Basic Medical Sciences, Jinan, China.
Yige WangDepartment of Biochemistry and Molecular Biology, Shandong University School of Basic Medical Sciences, Jinan, China.
Lijuan MaDepartment of Biochemistry and Molecular Biology, Shandong University School of Basic Medical Sciences, Jinan, China.
Lulu GuoDepartment of Biochemistry and Molecular Biology, Shandong University School of Basic Medical Sciences, Jinan, China.
Xinyue WuDepartment of Biochemistry and Molecular Biology, Shandong University School of Basic Medical Sciences, Jinan, China.
Xiaoyan LinDepartment of Pathology, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, China.
Pengju ZhangDepartment of Biochemistry and Molecular Biology, Shandong University School of Basic Medical Sciences, Jinan, China.ORCID 0000-0002-6643-0017
Shandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Deubiquitinating enzymes (DUBs) serve to maintain cellular homeostasis via protein ubiquitination and exert diverse regulatory functions in cancers and other diseases. Much progress has been made in characterizing biological roles of DUBs over the decades, yet the specific functions of many subclass members remain largely unexplored. It was not until recent years that the role of ubiquitin-specific-processing protease 35 (USP35) in cancers began to be understood. Here, we focus on delineating the roles and underlying mechanisms of USP35 in non-small cell lung cancer (NSCLC). The isobaric tags for relative and absolute quantitation (iTRAQ) comparative proteomic approach were employed to identify differentially expressed proteins (DEPs) in H1299 cells induced by USP35 overexpression or silencing. Among the potential interactome of USP35, ribosome-binding protein 1 (RRBP1), a membrane-bound protein in endoplasmic reticulum (ER), captured our attentions. RRBP1 expression was found to positively correlate with USP35 levels in both genetically modified cells and human NSCLC tissues. Concordantly, both RRBP1 expression and USP35 expression were found to positively correlate with poor prognoses in lung adenocarcinoma patients. At the molecular level, USP35 was verified to directly interact with RRBP1 to prevent it from proteasomal-dependent degradation. Functionally, USP35 alleviated ER stress-induced cell apoptosis by stabilizing RRBP1 in NSCLC cells. Collectively, these findings indicate that USP35 plays a critical role in resisting ER stress-induced cell death through deubiquitinating RRBP1, hence providing a rationale to target the USP35-RRBP1 axis as an alternative therapeutic option for NSCLC.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsApoptosisCarrier ProteinsEndopeptidasesEndoplasmic Reticulum StressHumansProteomicsCarrier ProteinsEndopeptidasesRRBP1 protein, humanUSP35 protein, humandeubiquitinating enzymesendoplasmic reticulum stressnon-small cell lung cancerribosome binding protein 1ubiquitin-specific-processing protease 35

Identifiers

PMID34618999
PMCPMC8978513
OpenAlexW3201673733

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.